ICTRP Search Portal

Main

Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	EUCTR
Last refreshed on:	17 March 2021
Main ID:	EUCTR2012-003065-17-HU
Date of registration:	18/09/2013
Prospective Registration:	Yes
Primary sponsor:	Novartis Pharma Services AG
Public title:	Study of efficacy and safety of everolimus and letrozole in estrogen receptor positive HER2 negative metastatic or locally advanced breast cancer patients.
Scientific title:	An open-label, phase II, single-arm study of everolimus in combination with letrozole in the treatment of postmenopausal women with estrogen receptor positive HER2 negative metastatic or locally advanced breast cancer
Date of first enrolment:	11/11/2013
Target sample size:	200
Recruitment status:	Not Recruiting
URL:	https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2012-003065-17
Study type:	Interventional clinical trial of medicinal product
Study design:	Controlled: no Randomised: no Open: Single blind: Double blind: Parallel group: Cross over: Other: If controlled, specify comparator, Other Medicinial Product: Placebo: Other:
Phase:	Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no

Countries of recruitment
Argentina	Austria	Brazil	France	Hungary	Japan	Korea, Republic of	Netherlands
Portugal	Spain	Thailand	Turkey	United Kingdom	United States

Contacts

Name:
Address:
Telephone:
Email:
Affiliation:

Name:
Address:
Telephone:
Email:
Affiliation:

Key inclusion & exclusion criteria

Inclusion criteria:
•Patients 18 years old or greater
•Patients with metastatic or locally advanced, unresectable breast cancer not amenable to curative treatment by surgery or radiotherapy
•Histological or cytological confirmation of estrogen-receptor positive (ER+) human epidermal growth factor receptor 2 negative (HER2-) breast cancer
•Postmenopausal women
•No prior treatment for metastatic breast cancer

Other protocol based inclusion criteria may apply
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 108
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 94

Exclusion criteria:
•Patients with only non-measurable lesions other than bone metastases (e.g., pleural effusion, ascites, etc)
•Patients who have received prior hormonal or any other systemic therapy for metastatic breast cancer.
•Patients may have received prior neoadjuvant or adjuvant endocrine therapy. In the case of neoadjuvant or adjuvant NSAI (letrozole/anastrozole) therapy patients must have completed therapy at least 1 year prior to study enrollment.
•Previous treatment with mTOR inhibitors.
•Known hypersensitivity to mTOR inhibitors, e.g., sirolimus (rapamycin).
•Other protocol-defined inclusion/exclusion criteria may apply

Other protocol based exclusion criteria may apply

Age minimum:
Age maximum:
Gender:
Female: yes
Male: no

Health Condition(s) or Problem(s) studied

Estrogen receptor positive metastatic breast cancer
MedDRA version: 20.0 Level: PT Classification code 10070577 Term: Oestrogen receptor positive breast cancer System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)

Therapeutic area: Diseases [C] - Cancer [C04]

Intervention(s)

Trade Name: Afinitor
Product Name: Everolimus
Product Code: RAD001
Pharmaceutical Form: Tablet
CAS Number: 159351-69-6
Current Sponsor code: RAD001
Other descriptive name: EVEROLIMUS
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 5-

Trade Name: Afinitor
Product Name: Everolimus
Product Code: RAD001
Pharmaceutical Form: Tablet
CAS Number: 159351-69-6
Current Sponsor code: RAD001
Other descriptive name: EVEROLIMUS
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 10-

Product Name: exemestane
Pharmaceutical Form: Coated tablet
INN or Proposed INN: exemestane
CAS Number: 107868-30-4
Other descriptive name: EXEMESTANE
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 25-

Product Name: Femara
Product Code: FEM345
Pharmaceutical Form: Tablet
INN or Proposed INN: LETROZOLE
CAS Number: 112809-51-5
Current Sponsor code: FEM345
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 2.5-

Primary Outcome(s)

Secondary Objective: - Determine the overall response rate and clinical benefit rate of everolimus + letrozole in the first line metastatic setting
- Determine the progression free survival and clinical benefit rate of everolimus + exemestane in second line population
- Estimate the overall survival of patients treated with everolimus + letrozole in the first line setting
- Evaluate a therapeutic intervention to reduce the severity and duration of stomatitis
- Evaluate the safety of everolimus + letrozole in the first line setting
- Evaluate the safety of everolimus + exemestane in the second line setting
- Evaluate clinical benefit as assessed by the investigator during the Extension Phase
- Evaluate long term safety data

Primary end point(s): Percentage of patients progression-free after completion of 1st line treatment (everolimus + letrozole)

Timepoint(s) of evaluation of this end point: 12 months after last patient recruited

Main Objective: The primary objective is to estimate progression-free survival in patients treated with everolimus + letrozole in the first line metastatic setting.

Secondary Outcome(s)

Secondary end point(s): - Overall response rate and clinical benefit rate in patients receiving the first line study treatment (everolimus + letrozole)
- Progression-free survival in the second line is defined as the time interval between start of 2nd line treatment and documented disease progression or death due to any cause reported during or after second-line treatment
- Overall survival of patients receiving first line study treatment (everolimus + letrozole)
- Reduction in severity and duration of oral stomatitis
- Assessment of safety based on the frequency of adverse events that fall outside normal pre-specified ranges
- Overall response rate and clinical benefit rate in patients receiving the second line study treatment (everolimus + exemestane)
- Reduction in severity and duration of oral stomatitis

Timepoint(s) of evaluation of this end point: - Baseline, every 8 weeks
- Baseline, every 8 weeks
- Continuous during the study and every 12 weeks after last treatment
- Upon onset of 1st stomatitis, patient will complete diary daily until resolution of stomatitis
- Continuous during the study, up to 28 days after last treatment
- Baseline, every 8 weeks
- Upon onset of 1st stomatitis and in countries where the alcohol-free dexamethasone solution (0.5mg/5ml) is commercially available, patient will be randomised to dexamethasone oral solution rinse or standard of care

Secondary ID(s)

2012-003065-17-GB

CRAD001Y24135

Source(s) of Monetary Support

Novartis Pharma Services AG

Secondary Sponsor(s)

Ethics review

Status: Approved
Approval date: 28/10/2013
Contact:

Results

Results available:
Date Posted:
Date Completed:
URL:

Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.